141 results on '"Lourenço, Delmar"'
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2. Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective study
3. Case Report: Composite pheochromocytoma with ganglioneuroma component: A report of three cases
4. A differential diagnosis of inherited endocrine tumors and their tumor counterparts
5. Supernumerary parathyroid glands in hyperparathyroidism associated with multiple endocrine neoplasia type 1
6. Post-surgical follow-up of primary hyperparathyroidism associated with multiple endocrine neoplasia type 1
7. Total parathyroidectomy in a large cohort of cases with hyperparathyroidism associated with multiple endocrine neoplasia type 1: experience from a single academic center
8. Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1
9. Narrowing the gap of personalized medicine in emerging countries: the case of multiple endocrine neoplasias in Brazil
10. Impact of parathyroidectomy on quality of life in multiple endocrine neoplasia type 1
11. Glucose-dependent insulinotropic peptide receptor overexpression in adrenocortical hyperplasia in MEN1 syndrome without loss of heterozygosity at the 11q13 locus
12. Isolated familial somatotropinoma: 11q13-loh and gene/protein expression analysis suggests a possible involvement of aip also in non-pituitary tumorigenesis
13. Hypercalcitoninemia is not Pathognomonic of Medullary Thyroid Carcinoma
14. Penetrance and Clinical Features of Pheochromocytoma in a Six-Generation Family Carrying a Germline TMEM127 Mutation
15. Sporadic Medullary Thyroid Carcinoma: Clinical Data From A University Hospital
16. Multiple Endocrine Neoplasia Type 1: Diagnosis, Management, and Treatment
17. Penetrance of Functioning and Nonfunctioning Pancreatic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1 in the Second Decade of Life
18. THE IMPACT OF CLINICAL AND GENETIC SCREENINGS ON THE MANAGEMENT OF THE MULTIPLE ENDOCRINE NEOPLASIA TYPE 1
19. Assessing the emerging oncogene protein kinase C epsilon as a candidate gene in families with Carney complex-2
20. Editorial: Early Genetic and Clinical Diagnosis in MEN1
21. Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy
22. High Penetrance of Pheochromocytoma Associated with the Novel C634Y/Y791F Double Germline Mutation in the RET Protooncogene
23. Germline Mutation in the Aryl Hydrocarbon Receptor Interacting Protein Gene in Familial Somatotropinoma
24. Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective study.
25. Impaired Adrenocorticotropin-Adrenal Axis in Combined Pituitary Hormone Deficiency Caused by a Two-Base Pair Deletion (301-302delAG) in the Prophet of Pit-1 Gene*
26. Giant Prolactinoma Causing Hydrocephalus and Intracranial Hypertension as First Manifestations of Multiple Endocrine Neoplasia Type 1
27. Quality of Life and Coping in Multiple Endocrine Neoplasia Type 2
28. Could the Less-Than Subtotal Parathyroidectomy Be an Option for Treating Young Patients With Multiple Endocrine Neoplasia Type 1-Related Hyperparathyroidism?
29. Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study
30. Less-than-subtotal parathyroidectomy as treatment for primary hyperparathyroidism in multiple endocrine neoplasia- type 1: a good option?
31. Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing
32. Preventive medicine of von Hippel–Lindau disease-associated pancreatic neuroendocrine tumors
33. 65 YEARS OF THE DOUBLE HELIX: Genetics informs precision practice in the diagnosis and management of pheochromocytoma
34. Questions and Controversies About Parathyroid Pathophysiology in Children With Multiple Endocrine Neoplasia Type 1
35. EPAS1 Mutations and Paragangliomas in Cyanotic Congenital Heart Disease
36. Correction: Familial Hyperparathyroidism – Disorders of Growth and Secretion in Hormone-Secretory Tissue
37. Assessment of Depression, Anxiety, Quality of Life, and Coping in Long-Standing Multiple Endocrine Neoplasia Type 2 Patients
38. Successful parathyroid tissue autograft after 3 years of cryopreservation: a case report
39. RET Y791F Variant Does Not Increase the Risk for Medullary Thyroid Carcinoma
40. Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility
41. Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations
42. Successful parathyroid tissue autograft after 3 years of cryopreservation: a case report
43. Early-onset, progressive, frequent, extensive, and severe bone mineral and renal complications in multiple endocrine neoplasia type 1-associated primary hyperparathyroidism
44. The Parathyroids and the Kidney: Fuller Albright Revisited
45. Complete Resolution of Hypercortisolism with Sorafenib in a Patient with Advanced Medullary Thyroid Carcinoma and Ectopic ACTH (Adrenocorticotropic Hormone) Syndrome.
46. Complete resolution of hypercortisolism with sorafenib in a patient with advanced medullary thyroid carcinoma and ectopic ACTH syndrome.
47. The Parathyroids and the Kidney: Fuller Albright Revisited.
48. Insights into the genetic landscape of pheochromocytomas and paragangliomas in a Brazilian cohort.
49. Doege-Potter syndrome associated to metastatic solitary fibrous tumor.
50. Familial Hyperparathyroidism - Disorders of Growth and Secretion in Hormone-Secretory Tissue.
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